ES2832883T3 - Procedimiento para la sustitución de un refrigerante de alto PCG por composiciones que comprenden HFC-1234yf - Google Patents
Procedimiento para la sustitución de un refrigerante de alto PCG por composiciones que comprenden HFC-1234yf Download PDFInfo
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- ES2832883T3 ES2832883T3 ES18154365T ES18154365T ES2832883T3 ES 2832883 T3 ES2832883 T3 ES 2832883T3 ES 18154365 T ES18154365 T ES 18154365T ES 18154365 T ES18154365 T ES 18154365T ES 2832883 T3 ES2832883 T3 ES 2832883T3
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- 239000000203 mixture Substances 0.000 title claims abstract description 208
- 239000003507 refrigerant Substances 0.000 title claims abstract description 105
- 238000000034 method Methods 0.000 title claims abstract description 91
- FXRLMCRCYDHQFW-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropene Chemical compound FC(=C)C(F)(F)F FXRLMCRCYDHQFW-UHFFFAOYSA-N 0.000 title claims abstract description 67
- RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 claims abstract description 80
- 238000005057 refrigeration Methods 0.000 claims abstract description 69
- 230000008569 process Effects 0.000 claims abstract description 61
- 238000004378 air conditioning Methods 0.000 claims abstract description 56
- GTLACDSXYULKMZ-UHFFFAOYSA-N pentafluoroethane Chemical compound FC(F)C(F)(F)F GTLACDSXYULKMZ-UHFFFAOYSA-N 0.000 claims abstract description 30
- UJPMYEOUBPIPHQ-UHFFFAOYSA-N 1,1,1-trifluoroethane Chemical compound CC(F)(F)F UJPMYEOUBPIPHQ-UHFFFAOYSA-N 0.000 claims abstract description 17
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 claims abstract description 15
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 claims abstract description 11
- MSSNHSVIGIHOJA-UHFFFAOYSA-N pentafluoropropane Chemical compound FC(F)CC(F)(F)F MSSNHSVIGIHOJA-UHFFFAOYSA-N 0.000 claims abstract description 8
- -1 butane or propane Chemical class 0.000 description 81
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- 150000001875 compounds Chemical class 0.000 description 28
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- 125000004122 cyclic group Chemical group 0.000 description 7
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- 229920006395 saturated elastomer Polymers 0.000 description 6
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- 125000002723 alicyclic group Chemical group 0.000 description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- 229910052801 chlorine Inorganic materials 0.000 description 5
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 5
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 5
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- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 5
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- 238000005461 lubrication Methods 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
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- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 5
- 150000003077 polyols Chemical class 0.000 description 5
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 4
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 4
- 125000004429 atom Chemical group 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
- 150000002170 ethers Chemical class 0.000 description 4
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 4
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- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
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- 229930195734 saturated hydrocarbon Natural products 0.000 description 4
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- UQRONKZLYKUEMO-UHFFFAOYSA-N 4-methyl-1-(2,4,6-trimethylphenyl)pent-4-en-2-one Chemical group CC(=C)CC(=O)Cc1c(C)cc(C)cc1C UQRONKZLYKUEMO-UHFFFAOYSA-N 0.000 description 3
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- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 3
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- 230000033228 biological regulation Effects 0.000 description 3
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- 125000002592 cumenyl group Chemical group C1(=C(C=CC=C1)*)C(C)C 0.000 description 3
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 3
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 3
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- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 3
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- NSGXIBWMJZWTPY-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)CC(F)(F)F NSGXIBWMJZWTPY-UHFFFAOYSA-N 0.000 description 2
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- 230000003647 oxidation Effects 0.000 description 1
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- GKASDNZWUGIAMG-UHFFFAOYSA-N triethyl orthoformate Chemical group CCOC(OCC)OCC GKASDNZWUGIAMG-UHFFFAOYSA-N 0.000 description 1
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- SZKKNEOUHLFYNA-UHFFFAOYSA-N undecanenitrile Chemical compound CCCCCCCCCCC#N SZKKNEOUHLFYNA-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M171/00—Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
- C10M171/008—Lubricant compositions compatible with refrigerants
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
- C08J9/143—Halogen containing compounds
- C08J9/144—Halogen containing compounds containing carbon, halogen and hydrogen only
- C08J9/146—Halogen containing compounds containing carbon, halogen and hydrogen only only fluorine as halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
- C08J9/149—Mixtures of blowing agents covered by more than one of the groups C08J9/141 - C08J9/143
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/02—Materials undergoing a change of physical state when used
- C09K5/04—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
- C09K5/041—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems
- C09K5/044—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds
- C09K5/045—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds containing only fluorine as halogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/12—Organic compounds only containing carbon, hydrogen and oxygen atoms, e.g. ketone or alcohol
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/14—Saturated hydrocarbons, e.g. butane; Unspecified hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/16—Unsaturated hydrocarbons
- C08J2203/162—Halogenated unsaturated hydrocarbons, e.g. H2C=CF2
-
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- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
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| EP3406686B1 (de) | 2005-03-04 | 2019-11-27 | The Chemours Company FC, LLC | Zusammensetzungen mit einem fluorolefin |
| US8628681B2 (en) | 2007-10-12 | 2014-01-14 | Mexichem Amanco Holding S.A. De C.V. | Heat transfer compositions |
| US8512591B2 (en) | 2007-10-12 | 2013-08-20 | Mexichem Amanco Holding S.A. De C.V. | Heat transfer compositions |
| GB201002625D0 (en) * | 2010-02-16 | 2010-03-31 | Ineos Fluor Holdings Ltd | Heat transfer compositions |
| US8333901B2 (en) | 2007-10-12 | 2012-12-18 | Mexichem Amanco Holding S.A. De C.V. | Heat transfer compositions |
| US8419968B2 (en) | 2008-11-13 | 2013-04-16 | Chemtura Corporation | Lubricants for refrigeration systems |
| WO2010085545A1 (en) | 2009-01-26 | 2010-07-29 | Chemtura Corporation | Production of polyol ester lubricants for refrigeration systems |
| IN2012DN02250A (de) | 2009-10-07 | 2015-08-21 | Chemtura Corp | |
| GB201002622D0 (en) | 2010-02-16 | 2010-03-31 | Ineos Fluor Holdings Ltd | Heat transfer compositions |
| CN102947409A (zh) | 2010-05-20 | 2013-02-27 | 墨西哥化学阿玛科股份有限公司 | 传热组合物 |
| GB2481443B (en) | 2010-06-25 | 2012-10-17 | Mexichem Amanco Holding Sa | Heat transfer compositions |
| GB2492847A (en) * | 2011-07-15 | 2013-01-16 | Mexichem Amanco Holding Sa | A process for reducing TFMA content in R-1234 |
| TWI682992B (zh) * | 2013-10-10 | 2020-01-21 | 杜邦股份有限公司 | 含二氟甲烷、五氟乙烷、及四氟丙烯的冷媒混合物及其用途 |
| US10330364B2 (en) | 2014-06-26 | 2019-06-25 | Hudson Technologies, Inc. | System and method for retrofitting a refrigeration system from HCFC to HFC refrigerant |
| WO2016075541A1 (en) | 2014-11-11 | 2016-05-19 | Kujak Stephen A | Refrigerant compositions and methods of use |
| US9556372B2 (en) * | 2014-11-26 | 2017-01-31 | Trane International Inc. | Refrigerant compositions |
| US10301521B2 (en) | 2016-07-29 | 2019-05-28 | Honeywell International Inc. | Heat transfer methods, systems and compositions |
| EP3717589A4 (de) * | 2017-11-30 | 2021-08-18 | Honeywell International Inc. | Wärmetransferzusammensetzungen, verfahren und systeme |
| KR102873124B1 (ko) * | 2018-01-30 | 2025-10-17 | 허니웰 인터내셔날 인코포레이티드 | 열 전달 조성물, 방법 및 시스템 |
| CN108384515A (zh) * | 2018-02-27 | 2018-08-10 | 湖北绿冷高科节能技术有限公司 | 一种替代r22的制冷剂 |
| CN109971433B (zh) * | 2019-04-08 | 2021-04-13 | 中国科学院理化技术研究所 | 一种多元混合制冷剂 |
| CN110845997B (zh) * | 2019-10-16 | 2020-12-22 | 珠海格力电器股份有限公司 | 一种热传递介质及适用于冷却器的组合物 |
| MX2023003388A (es) * | 2020-11-20 | 2023-03-31 | Chemours Co Fc Llc | Composiciones refrigerantes y usos de estas. |
| CN113980650B (zh) * | 2021-11-15 | 2023-09-08 | 太原理工大学 | 一种适配制冷热泵系统的制冷剂 |
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| WO2025264761A1 (en) * | 2024-06-21 | 2025-12-26 | The Chemours Company Fc, Llc | Compositions comprising fluoroolefins and natural refrigerants and uses thereof |
Family Cites Families (52)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US606855A (en) | 1898-07-05 | Roller-machine for forming round can-bodies | ||
| US3884828A (en) * | 1970-10-15 | 1975-05-20 | Dow Corning | Propellants and refrigerants based on trifluoropropene |
| US3723318A (en) * | 1971-11-26 | 1973-03-27 | Dow Corning | Propellants and refrigerants based on trifluoropropene |
| US5149453A (en) * | 1985-02-25 | 1992-09-22 | H. B. Fuller Automotive Products, Inc. | Method for detecting leakage in a refrigeration system |
| JPH04110388A (ja) * | 1990-08-31 | 1992-04-10 | Daikin Ind Ltd | 熱伝達用流体 |
| US5722256A (en) | 1990-12-17 | 1998-03-03 | E. I. Du Pont De Nemours And Company | Air conditioner and heat pump with tetrafluoroethane-containing working fluid |
| US5759430A (en) | 1991-11-27 | 1998-06-02 | Tapscott; Robert E. | Clean, tropodegradable agents with low ozone depletion and global warming potentials to protect against fires and explosions |
| JP3463303B2 (ja) | 1991-12-27 | 2003-11-05 | 日産自動車株式会社 | 車両用ヒートポンプ式冷暖房装置 |
| US6214624B1 (en) | 1992-12-31 | 2001-04-10 | Shell Oil Company | Use of perfluorocarbons as tracers in chemical compositions |
| US5611210A (en) | 1993-03-05 | 1997-03-18 | Ikon Corporation | Fluoroiodocarbon blends as CFC and halon replacements |
| USRE36951E (en) | 1994-08-29 | 2000-11-14 | Spectronics Corporation | Method of introducing leak detection dye into an air conditioning or refrigeration system including solid or semi-solid fluorescent dyes |
| RU2073058C1 (ru) | 1994-12-26 | 1997-02-10 | Олег Николаевич Подчерняев | Озонобезопасная рабочая смесь |
| JPH0967280A (ja) * | 1995-09-01 | 1997-03-11 | Daikin Ind Ltd | １，１，１，３，３−ペンタフルオロプロペンの製造方法及び１，１，１，３，３−ペンタフルオロプロパンの製造方法 |
| JP3781147B2 (ja) | 1997-04-09 | 2006-05-31 | カルソニックカンセイ株式会社 | ヒートポンプ式自動車用空気調和装置 |
| JPH11388A (ja) | 1997-06-12 | 1999-01-06 | Nippon Mizushiyori Giken:Kk | 消臭抗菌粉材 |
| US5811603A (en) * | 1997-12-01 | 1998-09-22 | Elf Atochem North America, Inc. | Gas phase fluorination of 1230za |
| WO1999062851A1 (en) | 1998-06-02 | 1999-12-09 | E.I. Du Pont De Nemours And Company | Processes for the production of hexafluoropropene and optionally other halogenated hydrocarbons containing fluorine |
| US6124510A (en) * | 1998-07-21 | 2000-09-26 | Elf Atochem North America, Inc. | 1234ze preparation |
| US6150306A (en) | 1999-03-04 | 2000-11-21 | Morton Internatioanl Inc. | Fluorescent tracer dyes |
| US6237357B1 (en) | 1999-06-07 | 2001-05-29 | Mitsubishi Heavy Industries, Ltd. | Vehicular air conditioner using heat pump |
| US6204405B1 (en) | 1999-12-22 | 2001-03-20 | Sigma-Aldrich Co. | Economical and convenient procedures for the synthesis of catecholborane |
| US7077960B2 (en) | 2000-03-07 | 2006-07-18 | Solvay (Societe Anonyme) | Method for obtaining a purified hydrofluoroalkane, purified hydrofluoroalkane, use of same and method for analysing same |
| FR2806077B1 (fr) † | 2000-03-07 | 2004-01-30 | Solvay | Procede pour l'obtention d'un hydrofluoroalcane epure, hydrofluoroalcane epure, utilisation de l'hydrofluoroalcane et methode d'analyse d'un hydrofluoroalcane |
| GB0010614D0 (en) * | 2000-05-04 | 2000-06-21 | Ici Plc | Removal of (hydro)haloalkene impurities from product streams |
| US6516837B2 (en) | 2000-09-27 | 2003-02-11 | Honeywell International Inc. | Method of introducing refrigerants into refrigeration systems |
| CN1137235C (zh) * | 2001-09-11 | 2004-02-04 | 顾雏军 | 在热力循环中使用的改进的非共沸工作介质 |
| US20040089839A1 (en) * | 2002-10-25 | 2004-05-13 | Honeywell International, Inc. | Fluorinated alkene refrigerant compositions |
| US7279451B2 (en) * | 2002-10-25 | 2007-10-09 | Honeywell International Inc. | Compositions containing fluorine substituted olefins |
| BRPI0315633B1 (pt) * | 2002-10-25 | 2020-11-10 | Honeywell International Inc. | composição de transferência de calor e método de transferir calor para ou a partir de um fluido ou corpo |
| US7524805B2 (en) | 2004-04-29 | 2009-04-28 | Honeywell International Inc. | Azeotrope-like compositions of tetrafluoropropene and hydrofluorocarbons |
| US7655610B2 (en) | 2004-04-29 | 2010-02-02 | Honeywell International Inc. | Blowing agent compositions comprising fluorinated olefins and carbon dioxide |
| US20050211949A1 (en) | 2003-11-13 | 2005-09-29 | Bivens Donald B | Detectable refrigerant compositions and uses thereof |
| US20050145822A1 (en) † | 2003-11-13 | 2005-07-07 | Drigotas Martin D. | Refrigerant compositions comprising UV fluorescent dye and solubilizing agent |
| WO2005067554A2 (en) | 2004-01-14 | 2005-07-28 | E.I. Dupont De Nemours And Company | Hydrofluorocarbon refrigerant compositions and uses thereof |
| US7276177B2 (en) | 2004-01-14 | 2007-10-02 | E.I. Dupont De Nemours And Company | Hydrofluorocarbon refrigerant compositions and uses thereof |
| US7641809B2 (en) † | 2004-02-26 | 2010-01-05 | E. I. Du Pont De Nemours And Company | Tracer-containing compositions |
| CN1954209A (zh) † | 2004-03-17 | 2007-04-25 | 索尔维公司 | 分析1,1,1,2－四氟乙烷的方法 |
| WO2005103191A2 (en) * | 2004-04-16 | 2005-11-03 | Honeywell International, Inc. | Azeotrope-like trifluoroiodomethane compositions |
| US7622435B2 (en) | 2004-04-16 | 2009-11-24 | Honeywell International Inc. | Methods of replacing refrigerant |
| US7098176B2 (en) | 2004-04-16 | 2006-08-29 | Honeywell International Inc. | Azeotrope-like compositions of tetrafluoropropene and pentafluoropropene |
| CA2564023C (en) | 2004-04-16 | 2012-07-17 | Honeywell International Inc. | Azeotrope-like compositions of tetrafluoropropene and trifluoroiodomethane |
| US6969701B2 (en) | 2004-04-16 | 2005-11-29 | Honeywell International Inc. | Azeotrope-like compositions of tetrafluoropropene and trifluoroiodomethane |
| KR20070011554A (ko) † | 2004-04-29 | 2007-01-24 | 허니웰 인터내셔널 인코포레이티드 | 1,3,3,3-테트라플루오로프로펜의 합성 방법 |
| JP4864880B2 (ja) | 2004-04-29 | 2012-02-01 | ハネウェル・インターナショナル・インコーポレーテッド | １，３，３，３−テトラフルオロプロペン及び２，３，３，３−テトラフルオロプロペンの合成方法 |
| US7413675B2 (en) | 2004-06-29 | 2008-08-19 | E.I. Dupont De Nemours And Company | Hydrocarbon refrigerant compositions and uses thereof |
| US20060030719A1 (en) | 2004-08-03 | 2006-02-09 | Fagan Paul J | Cis-3,5-disubstituted-dihydro-furan-2-ones and the preparation and use thereof |
| EP3406686B1 (de) | 2005-03-04 | 2019-11-27 | The Chemours Company FC, LLC | Zusammensetzungen mit einem fluorolefin |
| US20060243944A1 (en) | 2005-03-04 | 2006-11-02 | Minor Barbara H | Compositions comprising a fluoroolefin |
| PL1951838T3 (pl) * | 2005-11-01 | 2013-12-31 | Du Pont | Kompozycje zawierające fluoroolefiny i ich zastosowania |
| CN102947409A (zh) | 2010-05-20 | 2013-02-27 | 墨西哥化学阿玛科股份有限公司 | 传热组合物 |
| US10224430B1 (en) | 2017-12-06 | 2019-03-05 | International Business Machines Corporation | Thin film transistors with epitaxial source/drain and drain field relief |
| DE102018113958B4 (de) † | 2018-06-12 | 2022-03-31 | Dr. Ing. H.C. F. Porsche Aktiengesellschaft | Kompaktes 2-Gang-Kraftfahrzeuggetriebe zur Ankoppelung einer elektrischen Maschine |
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